Canonical Allele Identifier: CA2497029082

Gene: DRD3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114144040G= , CM000665.2:g.114144040G=	GRCh38
NC_000003.11:g.113862887G= , CM000665.1:g.113862887G=	GRCh37
NC_000003.10:g.115345577G=	NCBI36
NG_008842.2:g.60368C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000796.6:c.526+3375C= MANE Select	NP_000787.2:n.526+3375C=
ENST00000383673.5:c.526+3375C= MANE Select	ENSP00000373169.2:n.526+3375C=
NM_000796.5:c.526+3375C=	NP_000787.2:n.526+3375C=
NM_001282563.2:c.526+3375C=	NP_001269492.1:n.526+3375C=
NM_001290809.1:c.526+3375C=	NP_001277738.1:n.526+3375C=
NM_033663.5:c.526+3375C=	NP_387512.3:n.526+3375C=
NM_033663.6:c.526+3375C=	NP_387512.3:n.526+3375C=
ENST00000295881.9:c.526+3375C=	ENSP00000295881.6:n.526+3375C=
ENST00000383673.4:c.526+3375C=	ENSP00000373169.2:n.526+3375C=
ENST00000460779.5:c.526+3375C=	ENSP00000419402.1:n.526+3375C=
ENST00000467632.5:c.526+3375C=	ENSP00000420662.1:n.526+3375C=
ENST00000698213.1:c.526+3375C=	ENSP00000513607.1:n.526+3375C=
XM_011512510.1:c.526+3375C=	XP_011510812.1:n.526+3375C=
XM_011512511.1:c.526+3375C=	XP_011510813.1:n.526+3375C=
XM_011512512.1:c.526+3375C=	XP_011510814.1:n.526+3375C=
XM_017005829.1:c.526+3375C=	XP_016861318.1:n.526+3375C=